Roel A. Ophoff
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Genomic variations and chromosomal abnormalities, Genetics and Neurodevelopmental Disorders, Genomics and Rare Diseases, Bipolar Disorder and Treatment
Most-Cited Works
- → Familial Hemiplegic Migraine and Episodic Ataxia Type-2 Are Caused by Mutations in the Ca2+ Channel Gene CACNL1A4(1996)2,331 cited
- → Large recurrent microdeletions associated with schizophrenia(2008)1,772 cited
- → Common variants conferring risk of schizophrenia(2009)1,708 cited
- → Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47(2011)1,348 cited
- → Multiple common variants for celiac disease influencing immune gene expression(2010)1,042 cited
- → Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium(2018)949 cited
- → Aging effects on DNA methylation modules in human brain and blood tissue(2012)671 cited
- → Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis(2016)620 cited
- → Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights(2018)548 cited
- → Subcortical volumetric abnormalities in bipolar disorder(2016)515 cited